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THIELAVIN-F;4-[4'-(2'',4''-DIHYDROXY-3'',6''-DIMETHYLBENZOYLOXY)-3',5',6'-TRIMETHYL-2'-METHOXYBENZOYLOXY]-2-METHOXY-5,6-DIMETHYLBENZOIC-ACID

Compound with spectra: 1 NMR

THIELAVIN-F;4-[4'-(2'',4''-DIHYDROXY-3'',6''-DIMETHYLBENZOYLOXY)-3',5',6'-TRIMETHYL-2'-METHOXYBENZOYLOXY]-2-METHOXY-5,6-DIMETHYLBENZOIC-ACID
SpectraBase Compound ID C08igSkoN3d
InChI InChI=1S/C30H32O10/c1-12-10-19(31)17(6)25(32)22(12)29(35)40-26-16(5)15(4)24(27(38-9)18(26)7)30(36)39-20-11-21(37-8)23(28(33)34)14(3)13(20)2/h10-11,31-32H,1-9H3,(H,33,34)
InChIKey DRJGKQRTLCMIRQ-UHFFFAOYSA-N
Mol Weight 552.6 g/mol
Molecular Formula C30H32O10
Exact Mass 552.199547 g/mol

View Spectrum of THIELAVIN-F;4-[4'-(2'',4''-DIHYDROXY-3'',6''-DIMETHYLBENZOYLOXY)-3',5',6'-TRIMETHYL-2'-METHOXYBENZOYLOXY]-2-METHOXY-5,6-DIMETHYLBENZOIC-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
THIELAVIN-J;4-[4'-(2'',4''-DIHYDROXY-3'',6''-DIMETHYLBENZOYLOXY)-3',5',6'-TRIMETHYL-2'-METHOXYBENZOYLOXY]-2-HYDROXY-3,6-DIMETHYLBENZOIC-ACID
THIELAVIN-G;4-[4'-(2'',4''-DIHYDROXY-3'',6''-DIMETHYLBENZOYLOXY)-5',6'-DIMETHYL-2'-METHOXYBENZOYLOXY]-2-METHOXY-3,5,6-TRIMETHYLBENZOIC-ACID
THIELAVIN-L;4-[4'-(2'',4''-DIHYDROXY-3'',6''-DIMETHYLBENZOYLOXY)-3',5',6'-TRIMETHYL-2'-METHOXYBENZOYLOXY]-2-HYDROXY-3,5,6-TRIMETHYLBENZOYLOXY-2'''',3''''-P
4''-HYDROXYSULFOXY_2,2''-DIMETHYLTHIELAVIN_P;4-(4'-(2''-METHOXY-4''-HYDROXYSULFOXY-3'',5'',6''-TRIMETHYLBENZYLOXY)-2'-HYDROXY-3',5',6'-TRIMETHYLBENZYLOXY
Benzoic acid, 3-chloro-2,5-dimethyl-4,6-bis(phenylmethoxy)-, 3-methoxy-4-(methoxycarbonyl)-2,5,6-trimethylphenyl ester
Benzoic acid, 3-chloro-2,5-dimethyl-4,6-bis(phenylmethoxy)-, 3-hydroxy-4-(methoxycarbonyl)-2,5,6-trimethylphenyl ester
THAMNOLINSAEURE
11H-Dibenzo[b,e][1,4]dioxepin-11-one, 3-hydroxy-8-methoxy-1,4,6,9-tetramethyl-
Methyl 4-(4'-benzyloxy-3'-chloro-6'-hydroxy-2'-methylbenzoyloxy)-2-hydroxy-5-methoxy-3,6-dimethylbenzoate
4,6-Diallylphomosine A
Title Journal or Book Year
Thielavins as Glucose-6-phosphatase (G6Pase) Inhibitors: Producing Strain, Fermentation, Isolation, Structural Elucidation and Biological Activities. The Journal of Antibiotics 2002
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